小泡
自组装
膜
纳米技术
纳米尺度
分子
纳米结构
材料科学
原细胞
化学
生物化学
有机化学
作者
James T. Kindt,Jack W. Szostak,Anna Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-06-30
卷期号:14 (11): 14627-14634
被引量:48
标识
DOI:10.1021/acsnano.0c03125
摘要
The desire to create cell-like models for fundamental science and applications has spurred extensive effort towards creating giant unilamellar vesicles (GUVs). However, a route to selectively self-assemble GUVs in bulk has remained elusive. In bulk solution, membrane-forming molecules such as phospholipids, single-tailed surfactants, and block copolymers typically self-assemble into multilamellar, onion-like structures. So although self-assembly processes can form nanoscale unilamellar vesicles, scaffolding by droplets or surfaces is required to create GUVs. Here we show that surprisingly, it is possible to bulk self-assemble cell-sized GUVs with almost complete selectivity over other vesicle topologies. The seemingly paradoxical pair of features that enables this appears to be having very dynamic molecules at the nanoscale, that create unusually rigid membranes. The resultant self-assembly pathway enables encapsulation of molecules and colloids, and can also generate model primitive cells that can grow and divide.
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